Assoc. Central Monitor, French Speaker

This is a fully remote position, open to applicants in Brazil, +5 more countries.

📋 Description

• Conduct centralized monitoring tasks for designated projects, assessing study quality and integrity in accordance with protocols, SOPs, regulations, and guidelines.

• Accurately maintain internal systems, databases, tracking tools, and project reports.

• Manage triggers and prepare i-site packs for assigned sites and countries.

• Assist with basic data analytics and perform trend analyses.

• Engage in study team meetings and collaborate with cross-functional staff to validate information and address data issues or action items.

• Report site quality concerns to the Centralized Monitoring Lead or Senior Central Monitor.

• Conduct subject-level data reviews and assess inclusion/exclusion criteria, investigational product, adverse events, laboratory results, endpoints, serious adverse events, and other patient information.

• Communicate with sites and Clinical Research Associates (CRAs) and follow up on study milestones from project initiation through to closeout.

• Provide backup support and execute delegated tasks assigned by the Central Monitor Expert or Centralized Monitoring Lead.

• Offer support to sites in North America and potentially in Latin America.

⛳️ Requirements

• Reside in Argentina, Brazil, Mexico, Peru, Colombia, or Chile.

• Bachelor's degree in life sciences or a related field, or a nursing qualification; or be nearing completion of the degree - Mandatory.

• For the Central Monitor role: a minimum of 2 years of monitoring experience (either on-site or remotely).

• For the Associate Central Monitor role: at least 2 years of study coordinator experience.

• Proficiency in English and French at an advanced level is mandatory; both languages will be assessed.

• Advanced Excel skills are required.

🏝️ Benefits

• Home-based position.